Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:57372343-57372498 | Rare:34 | ||||
chr16:57447326-57447536 | Common:2; Rare:62; Clinvar:2; Clinvar (benign):3 | ||||
chr16:57536567-57536853 | Common:4; Rare:76 | ||||
chr16:57619565-57619782 | Common:2; Rare:44 | ||||
chr16:57619935-57620133 | Rare:43 | ||||
chr16:57628530-57628730 | Common:4; Rare:52 | ||||
chr16:57668229-57668330 | Common:1; Rare:22 | ||||
chr16:57797937-57798249 | Rare:111 | ||||
chr16:57984906-57985240 | Common:5; Rare:109 | ||||
chr16:58000522-58000797 | Common:2; Rare:67 | ||||
chr16:58001310-58001472 | Rare:47 | ||||
chr16:58129274-58129570 | Common:3; Rare:95 | ||||
chr16:58392824-58392898 | Rare:18 | ||||
chr16:58515405-58515538 | Common:2; Rare:53 | ||||
chr16:58629751-58630112 | Common:2; Rare:96 |